4.6 Article

Stereoselective Four-Component Synthesis of Functionalized 2,3-Dihydro-4-Nitropyrroles

Journal

FRONTIERS IN CHEMISTRY
Volume 7, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fchem.2019.00810

Keywords

multicomponent reaction; ketoamide; heterocycles; nitro; dihydropyrroles; cascade reaction; 1,5-dipolar cyclization

Funding

  1. National Natural Science Foundation of China [81673296]

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We report a metal-free and stereoselective four-component reaction between alpha-ketoamides, amines, aromatic aldehydes and beta-nitroalkenes or beta-pivaloxy-nitroalkanes to obtain 2,3-dihydro-4-nitropyrroles functionalized in every position. The heterocycles accessible using this reaction may have utility in the synthesis of pharmacologically active compounds.

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